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65 Possible Causes for Deafness, Sensorineural Hearing Loss May Be Presenting Feature

  • Congenital Deafness

    Congenital deafness is either genetically caused or acquired in utero through maternal lifestyle and/or infection.[symptoma.com] Features may range from those with classical Pendred syndrome presenting with goitre and prelingual profound sensorineural hearing loss, to those with absence of goitre, normal[bmb.oxfordjournals.org] The methods by which congenital deafness soon may be diagnosed and the implications for the otologist are discussed.[ncbi.nlm.nih.gov]

  • Susac Syndrome

    It is clinically characterized by a typical triad of sensorineural deafness, encephalopathy, and visual defect, due to microangiopathy involving the brain, inner ear, and[ncbi.nlm.nih.gov] […] to retinal branch occlusions, and sensorineural hearing loss.[ncbi.nlm.nih.gov] Audiogram revealed severe bilateral deafness, according to the literature [ 4 ].[panafrican-med-journal.com]

  • Otosclerosis

    In the preliminary stages, the individuals suffer from partial hear loss which gets worse over time and results in complete deafness.[symptoma.com] hearing loss.[ncbi.nlm.nih.gov] Profound deafness has received increasing attention in recent years, largely because of the availability of cochlear implants.[ncbi.nlm.nih.gov]

  • Primary Optic Atrophy

    The severe form is usually detected in infancy or earlier because of macrocephaly, hepatosplenomegaly, deafness, blindness, severe anemia, leucopenia, and thrombocytopenia[djo.org.in] Twenty per cent develop sensorineural hearing loss; other features are less common. 22. Behr syndrome Inheritance is AR; heterozygotes may have mild features.[slideshare.net] Tay-Sachs Niemann-Pick Mucopolysaccharidoses Other inherited neurodegenerative conditions Wolfram syndrome (DIDMOAD: diabetes insipidus, diabetes mellitus, optic atrophy, and deafness[unboundmedicine.com]

  • Alstrom Syndrome

    It is characterized by retinal pigment degeneration, obesity, sensorineural deafness, non-insulin-dependent diabetes mellitus, progressive chronic nephropathy, cardiomyopathy[ncbi.nlm.nih.gov] […] in infancy or adolescence. 3 , 5 Other features that may present are short stature, bladder instability, chronic renal and hepatic dysfunction, early-onset type 2 diabetes[pediatrics.aappublications.org] Total blindness and deafness are likely to develop. Did you find this information useful?[patient.info]

  • Autosomal Dominant Deafness 11

    […] transplantation in a Parkinson rat model. ‎ 108 ページ - Mutation in mitochondrial tRNAIeu (UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness[books.google.com] Features may range from those with classical Pendred syndrome presenting with goitre and prelingual profound sensorineural hearing loss, to those with absence of goitre, normal[academic.oup.com] deafness type DFNA Autosomal dominant isolated sensorineural hearing loss type DFNA Autosomal dominant non-syndromic neurosensory deafness type DFNA Autosomal dominant non-syndromic[orpha.net]

  • Autosomal Recessive Deafness 84B

    Genetics of Deafness, written by leading authors in the field, is a must read for clinicians, researchers, and students.[books.google.de] Features may range from those with classical Pendred syndrome presenting with goitre and prelingual profound sensorineural hearing loss, to those with absence of goitre, normal[academic.oup.com] […] for Deafness Causes See also causal information: Causes of Deafness • • • References Source: GTR (NCBI/NIH): ncbi.nlm.nih.gov/ gtr/ conditions/ C3554159/ • • • Note: This[familydiagnosis.com]

  • Autosomal Recessive Deafness 76

    Genetics of Deafness, written by leading authors in the field, is a must read for clinicians, researchers, and students.[books.google.de] Features may range from those with classical Pendred syndrome presenting with goitre and prelingual profound sensorineural hearing loss, to those with absence of goitre, normal[academic.oup.com] Format Definition A form of non-syndromic sensorineural deafness, a disorder resulting from damage to the neural receptors of the inner ear, the nerve pathways to the brain[uniprot.org]

  • Cryopyrin-Associated Periodic Syndrome

    Seven patients (54%) had sensorineural deafness. Nine patients (69%) reported myalgia. Six patients (46%) had papilledema and a further 2 (15%) had optic disc pallor.[ncbi.nlm.nih.gov] Characteristically Muckle-Wells syndrome is associated with the early development of progressive sensorineural hearing loss.[dermnetnz.org] Deafness or partial hearing loss often develops by teenage years, and, if untreated, it may lead to amyloidosis.[rheumatology.org]

  • Autosomal Dominant Deafness 64

    Test Cost : 3000.00 AED Reporting Time: 5 Week Sample Type: EDTA blood or DNA Deafness autosomal dominant type 64 (DIABLO) Test Description : Deafness autosomal dominant type[dnalabsuae.com] Features may range from those with classical Pendred syndrome presenting with goitre and prelingual profound sensorineural hearing loss, to those with absence of goitre, normal[academic.oup.com] DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial[en.wikipedia.org]

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